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Chewing Capability Study for Infants and Toddlers

Effect of Food Structural Properties on Infants and Toddlers Mastication Abilities

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02156986
Enrollment
68
Registered
2014-06-05
Start date
2013-10-31
Completion date
2014-07-31
Last updated
2014-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

The main objective of the study is to conduct a pilot study on the characterization of the mastication abilities of infants and toddlers using different commercial cereal based products in order to gain knowledge and be able to plan future studies.

Interventions

None listed

Sponsors

Société des Produits Nestlé (SPN)
Lead SponsorINDUSTRY

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
9 Months to 36 Months
Healthy volunteers
Yes

Inclusion criteria

* Born at term (37+ weeks) * Familiar with solid foods * No known history of food allergies * Child must be within 2 weeks of the targeted age group for 9 months, within 1 month for 12 months, within 2 months for 18 and 24 months, and within 3 months for 36 months for this study. * English must be the primary language of the participant and family. * Having obtained his/her caregiver's or legal representative's informed consent.

Exclusion criteria

* History of speech/language, cognitive, or physical impairments as indicated on the self-reported medical history questionnaire completed by caregiver or legal guardian * Any previously undiagnosed speech/language or cognitive impairment detected by the Investigator. In the case a subject is identified as being at risk for a communication or feeding impairment, the caregiver will be notified and provided with a list of local speech-language pathology providers who could perform a formal assessment * History of poor weight gain/ weight loss, food allergies, difficulties with sucking, difficulties with chewing and/ or swallowing, frequent drooling (for age groups 18, 24, and 36 months), frequent choking, gastro-esophageal reflux, frequent spitting up/ vomiting (for age groups 18, 24, and 36 months) or irritability after feedings/ eating * Latex allergies * Currently participating in or having participated in a similar clinical trial related to food/diet within the last 9 months * Caregiver must not be under the age of 18 years old.

Design outcomes

Primary

MeasureTime frame
Muscle activities involved in the mastication using Electromyography (EMG)One day during the study visit 2

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026